Large granular lymphocytic leukemia complicating autoimmune polyglandular syndrome type 1 in siblings

Autoimmune polyglandular syndrome type 1 (APS1) is a rare autosomal recessive disorder, and large granular lymphocytic leukemia (LGLL) may, even more rarely, complicate APS1. LGLL may be subtle in presentation, but it is imperative to recognize LGLL in APS1 promptly, as outcome may otherwise be fata...

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Detalles Bibliográficos
Autores principales: Harrison, Jonathan S., Parmar, Harsh, Wang, Xiangbing D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930195/
https://www.ncbi.nlm.nih.gov/pubmed/29744070
http://dx.doi.org/10.1002/ccr3.1454
Descripción
Sumario:Autoimmune polyglandular syndrome type 1 (APS1) is a rare autosomal recessive disorder, and large granular lymphocytic leukemia (LGLL) may, even more rarely, complicate APS1. LGLL may be subtle in presentation, but it is imperative to recognize LGLL in APS1 promptly, as outcome may otherwise be fatal, as described herein.

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